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Synlett 2016; 27(09): 1438-1442
DOI: 10.1055/s-0035-1561373
DOI: 10.1055/s-0035-1561373
letter
Metal-Free Amidation of Ethers with N,N-Dibromosulfonamides
Weitere Informationen
Publikationsverlauf
Received: 04. Dezember 2015
Accepted after revision: 15. Januar 2016
Publikationsdatum:
08. Februar 2016 (online)
![](https://www.thieme-connect.de/media/synlett/201609/lookinside/thumbnails/st-2015-w0942-l_10-1055_s-0035-1561373-1.jpg)
Abstract
A new metal-free amidation of ethers with N,N-dibromosulfonamides has been developed. A series of hemiaminal ethers or imines were prepared with moderate to good yields.
Key words
amidation - amides - N,N-dibromosulfonamides - ethers - hemiaminal ethers - nitrene - regioselectivitySupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1561373.
- Supporting Information
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For selected reviews on amination reaction, see:
For selected reviews on nitrene chemistry, see:
For selected examples, see:
For selected examples on photoinduced radical strategy, see:
For selected examples of oxidative cross-dehydrogenative-coupling strategy, see:
For selected examples, see: